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Sr. Clinical Research Associate(m/w/x)
Site qualification, initiation, monitoring, and close-out visits for trials at a global clinical research organization. Minimum 2 years CRA experience and in-depth ICH-GCP knowledge required. Frequent site travel expected.
Requirements
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years Clinical Research Associate experience
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational, communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Tasks
- Conduct clinical trial site qualification visits.
- Conduct clinical trial site initiation visits.
- Conduct clinical trial site monitoring visits.
- Conduct clinical trial site close-out visits.
- Ensure protocol compliance in clinical trials.
- Ensure data integrity in clinical trials.
- Ensure patient safety in clinical trials.
- Collaborate with investigators and site staff.
- Facilitate smooth study conduct.
- Review clinical data for quality.
- Resolve clinical data queries for quality.
- Prepare study documentation.
- Review study documentation.
- Prepare study protocols.
- Review study protocols.
- Prepare clinical study reports.
- Review clinical study reports.
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
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Sr. Clinical Research Associate(m/w/x)
Site qualification, initiation, monitoring, and close-out visits for trials at a global clinical research organization. Minimum 2 years CRA experience and in-depth ICH-GCP knowledge required. Frequent site travel expected.
Requirements
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years Clinical Research Associate experience
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational, communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Tasks
- Conduct clinical trial site qualification visits.
- Conduct clinical trial site initiation visits.
- Conduct clinical trial site monitoring visits.
- Conduct clinical trial site close-out visits.
- Ensure protocol compliance in clinical trials.
- Ensure data integrity in clinical trials.
- Ensure patient safety in clinical trials.
- Collaborate with investigators and site staff.
- Facilitate smooth study conduct.
- Review clinical data for quality.
- Resolve clinical data queries for quality.
- Prepare study documentation.
- Review study documentation.
- Prepare study protocols.
- Review study protocols.
- Prepare clinical study reports.
- Review clinical study reports.
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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